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Systemic capsaicin inhibits neuronal activation in the brainstem during postoperative ileus in the mouse.

作者信息

Mueller Mario H, Kampitoglou Dimitrios, Glatzle Joerg, Hahn Jutta, Kreis Martin E

机构信息

Department of Surgery, Ludwig-Maximilian University, Munich, Germany.

出版信息

Langenbecks Arch Surg. 2006 Apr;391(2):88-95. doi: 10.1007/s00423-006-0042-8. Epub 2006 Mar 30.


DOI:10.1007/s00423-006-0042-8
PMID:16572327
Abstract

INTRODUCTION: Neuronal inhibitory reflex mechanisms contribute to postoperative ileus after abdominal surgery. During this condition, sensory neurons in the brainstem are activated. We aimed to determine the contribution of capsaicin-sensitive afferents to central vagal sensitivity in mice during postoperative ileus. MATERIALS AND METHODS: Under enflurane anesthesia, C57BL/6 mice were laparotomized and the small bowel was manipulated to induce ileus or was left untouched as a sham-treatment group. A subgroup of ileus animals was pre-treated with Capsaicin (1 microm/kg, i.p.) 48 h before small bowel manipulation. The animals were killed 24 h later and the brainstem was removed for Fos immunohistochemistry, which was quantified in the nucleus of the solitary tract (nTS). Spontaneous jejunal motility was recorded in vitro. Leukocyte infiltration in the intestinal muscularis was studied by myeloperoxidase staining as an index of postoperative inflammation. RESULTS: There were 30+/-9 Fos-positive neurons counted in the nTS after ileus and 6+/-2 in sham controls (Bregma -7.70 mm, P=0.01). A reduction to 8+/-3 was observed after Capsaicin pre-treatment in ileus animals (P<0.05). Peak amplitudes of spontaneous jejunal motility were 2+/-0.3 cmH2O during postoperative ileus, 3+/-0.6 cmH2O after ileus with capsaicin pre-treatment, and 10+/-2 cmH2O in control animals (N=6, both P<0.05). The number of leukocytes infiltrating the muscularis was 39+/-9/mm2 during ileus and 1.8+/-1/mm2 in controls (mean+/-SEM, P<0.01, N=6). After capsaicin, this number increased to 72+/-28/mm2 in ileus animals (P<0.05 vs control animals, N=7). CONCLUSION: The inhibition of capsaicin-sensitive vagal afferent pathways appears to boost rather than to attenuate the inflammatory response during postoperative ileus, while intestinal motility remained unchanged. This suggests a protective role of the capsaicin-sensitive afferent innervation for the inflammatory phase of postoperative ileus.

摘要

相似文献

[1]
Systemic capsaicin inhibits neuronal activation in the brainstem during postoperative ileus in the mouse.

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[2]
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[6]
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[7]
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[8]
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引用本文的文献

[1]
Patterns of Brain Activation and Meal Reduction Induced by Abdominal Surgery in Mice and Modulation by Rikkunshito.

PLoS One. 2015-9-30

[2]
Capsaicin-sensitive vagal afferent neurons contribute to the detection of pathogenic bacterial colonization in the gut.

J Neuroimmunol. 2013-3-5

[3]
Vagal innervation and early postoperative ileus in mice.

J Gastrointest Surg. 2011-3-25

本文引用的文献

[1]
The mechanisms of immune-to-brain communication in inflammation as a drug target.

Curr Drug Targets Inflamm Allergy. 2002-9

[2]
Postoperative ileus is maintained by intestinal immune infiltrates that activate inhibitory neural pathways in mice.

Gastroenterology. 2003-10

[3]
Neuroanatomy of visceral nociception: vagal and splanchnic afferent.

Gut. 2002-7

[4]
Preoperative intraluminal application of capsaicin increases postoperative gastric and colonic motility in rats.

J Gastrointest Surg. 2001

[5]
The diversity in the vanilloid (TRPV) receptor family of ion channels.

Trends Pharmacol Sci. 2002-4

[6]
Intraperitoneal capsaicin treatment reduces postoperative gastric ileus in awake rats.

Langenbecks Arch Surg. 2001-4

[7]
Vagus nerve stimulation attenuates the systemic inflammatory response to endotoxin.

Nature. 2000-5-25

[8]
Sense and specificity: a molecular identity for nociceptors.

Curr Opin Neurobiol. 1999-10

[9]
Surgically induced leukocytic infiltrates within the rat intestinal muscularis mediate postoperative ileus.

Gastroenterology. 1999-8

[10]
Intragastric capsaicin stimulates motility of upper gut and proximal colon via distinct pathways in conscious dogs.

Dig Dis Sci. 1999-6

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